The following data is part of a premarket notification filed by Microtech Medical Systems, Inc. with the FDA for Quadra-titer I.d..
| Device ID | K860208 |
| 510k Number | K860208 |
| Device Name: | QUADRA-TITER I.D. |
| Classification | Kit, Identification, Enterobacteriaceae |
| Applicant | MICROTECH MEDICAL SYSTEMS, INC. 401 LAREDO ST., UNIT 1 Aurora, CO 80011 |
| Contact | Jerry G Kilgore |
| Correspondent | Jerry G Kilgore MICROTECH MEDICAL SYSTEMS, INC. 401 LAREDO ST., UNIT 1 Aurora, CO 80011 |
| Product Code | JSS |
| CFR Regulation Number | 866.2660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-01-22 |
| Decision Date | 1986-03-03 |